Dual targeting of HER2-positive cancer with trastuzumab-emtansine (T- DM1) and pertuzumab: critical role for neuregulin blockade in anti-tumor response to combination therapy

نویسندگان

  • Gail D. Lewis
  • Carter T. Fields
  • Guangmin Li
  • Donald Dowbenko
  • Gabriele Schaefer
  • Kathy Miller
  • Fabrice Andre
  • Howard A. Burris
  • Kathy S. Albain
  • Nadia Harbeck
  • Veronique Dieras
  • Diana Crivellari
  • Liang Fang
  • Ellie Guardino
  • Steven R. Olsen
  • Lisa M. Crocker
  • Mark X. Sliwkowski
چکیده

Authors’ Affiliations: Research Oncology, Genentech, Inc., South San Francisco, CA; Indiana University Simon Cancer Center, Indianapolis, IN; Institute Gustave Roussy, Villejuif, France; Sarah Cannon Research Institute, Nashville, TN; Loyola University Medical Center, Maywood, IL; University of Cologne Breast Center, Cologne, Germany; Department of Medical Oncology, Institut Curie, Paris, France; Division of Medical Oncology, Centro di Riferimento Oncologico, Instituto Nazionale Tumori Aviano, Italy; Department of Biostatistics, Department of Product Development Oncology, Department of Translational Oncology, Genentech, Inc., South San Francisco, CA; *contributed equally to this work.

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منابع مشابه

Dual targeting of HER2-positive cancer with trastuzumab emtansine and pertuzumab: critical role for neuregulin blockade in antitumor response to combination therapy.

PURPOSE Targeting HER2 with multiple HER2-directed therapies represents a promising area of treatment for HER2-positive cancers. We investigated combining the HER2-directed antibody-drug conjugate trastuzumab emtansine (T-DM1) with the HER2 dimerization inhibitor pertuzumab (Perjeta). EXPERIMENTAL DESIGN Drug combination studies with T-DM1 and pertuzumab were performed on cultured tumor cells...

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Purpose: Targeting HER2 with multiple HER2-directed therapies represents a promising area of treatment for HER2-positive cancers. We investigated combining the HER2-directed antibody–drug conjugate trastuzumab emtansine (T-DM1) with the HER2 dimerization inhibitor pertuzumab (Perjeta). Experimental Design: Drug combination studies with T-DM1 and pertuzumab were performed on cultured tumor cells...

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Trastuzumab Emtansine With or Without Pertuzumab Versus Trastuzumab Plus Taxane for Human Epidermal Growth Factor Receptor 2–Positive, Advanced Breast Cancer: Primary Results From the Phase III MARIANNE Study

Purpose Trastuzumab and pertuzumab are human epidermal growth factor receptor 2 (HER2) -targeted monoclonal antibodies, and trastuzumab emtansine (T-DM1) is an antibody-drug conjugate that combines the properties of trastuzumab with the cytotoxic activity of DM1. T-DM1 demonstrated encouraging efficacy and safety in a phase II study of patients with previously untreated HER2-positive metastatic...

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Enhanced antitumor activity of trastuzumab emtansine (T-DM1) in combination with pertuzumab in a HER2-positive gastric cancer model.

Human epidermal growth factor receptor 2 (HER2)-targeted therapy by trastuzumab has become increasingly important for treating HER2-positive cancers, and trastuzumab emtansine (T-DM1) is expected to serve as an effective alternative to trastuzumab. Pertuzumab, a HER2 dimerization inhibitor, showed prolonged progression-free survival when used with trastuzumab for HER2-positive breast cancer. In...

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T-DM1 Activity in Metastatic Human Epidermal Growth Factor Receptor 2-Positive Breast Cancers That Received Prior Therapy With Trastuzumab and Pertuzumab.

Purpose Ado-trastuzumab emtansine (T-DM1) is currently approved for treatment in patients with human epidermal growth factor receptor 2 (HER2)-positive, metastatic breast cancer (MBC) who previously received trastuzumab and a taxane. However, there are no data on the activity of T-DM1 in patients who received prior pertuzumab, which is now included as standard first-line therapy. The goal of th...

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تاریخ انتشار 2013